The following data is part of a premarket notification filed by Bio-vascular, Inc. with the FDA for Peri-strips.
Device ID | K940205 |
510k Number | K940205 |
Device Name: | PERI-STRIPS |
Classification | Mesh, Surgical |
Applicant | BIO-VASCULAR, INC. 2670 PATTON RD. Saint Paul, MN 55113 |
Contact | Bruce A Mcfarlane |
Correspondent | Bruce A Mcfarlane BIO-VASCULAR, INC. 2670 PATTON RD. Saint Paul, MN 55113 |
Product Code | FTM |
CFR Regulation Number | 878.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-01-14 |
Decision Date | 1994-05-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERI-STRIPS 74470478 1897944 Dead/Cancelled |
Bio-Vascular, Inc. 1993-12-17 |